A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6188017



Internal ID9165420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:151261434..151264518hg38UCSC Ensembl
Outerchr6:151261277..151264671hg38UCSC Ensembl
Innerchr6:151582569..151585653hg19UCSC Ensembl
Outerchr6:151582412..151585806hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg383395
hg193395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663585
Supporting Variants
SamplesHG01051
Known GenesAKAP12
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6188017
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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